Cole William G
Division of Orthopaedics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Clin Orthop Relat Res. 2002 Aug(401):6-16. doi: 10.1097/00003086-200208000-00003.
Considerable progress has been made in many aspects of osteogenesis imperfecta. The international Sillence classification of osteogenesis imperfecta is being expanded to include a greater range of subgroups of patients. Attempts are being made to identify the genes causing forms of osteogenesis imperfecta and related syndromes that are not caused by mutations of the Type I collagen genes. In medium-term studies, bisphosphonate treatment has been shown to be the first method of treatment to improve the clinical course of the disease significantly. Somatic cell therapy, using allogeneic bone marrow and mesenchymal stromal cell transplantation, are in their early phases of development for use in humans with osteogenesis imperfecta. Somatic gene therapy, which aims to inactivate the mutation, is being evaluated in laboratory and animal studies.
成骨不全症在许多方面都取得了显著进展。国际上对成骨不全症的席尔恩斯分类正在扩大,以纳入更多类型的患者亚组。人们正在努力确定导致成骨不全症及相关综合征的基因,这些病症并非由I型胶原蛋白基因突变引起。在中期研究中,双膦酸盐治疗已被证明是第一种能显著改善该病临床病程的治疗方法。使用异体骨髓和间充质基质细胞移植的体细胞疗法,正处于用于人类成骨不全症治疗的早期开发阶段。旨在使突变失活的体细胞基因疗法正在实验室和动物研究中进行评估。